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Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy

Motor neuron physiology and development depend on a continuous and tightly regulated trophic support from a variety of cellular sources. Trophic factors guide the generation and positioning of motor neurons during every stage of the developmental process. As well, they are involved in axon guidance...

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Autores principales: Tovar-y-Romo, Luis B., Ramírez-Jarquín, Uri Nimrod, Lazo-Gómez, Rafael, Tapia, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937589/
https://www.ncbi.nlm.nih.gov/pubmed/24616665
http://dx.doi.org/10.3389/fncel.2014.00061
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author Tovar-y-Romo, Luis B.
Ramírez-Jarquín, Uri Nimrod
Lazo-Gómez, Rafael
Tapia, Ricardo
author_facet Tovar-y-Romo, Luis B.
Ramírez-Jarquín, Uri Nimrod
Lazo-Gómez, Rafael
Tapia, Ricardo
author_sort Tovar-y-Romo, Luis B.
collection PubMed
description Motor neuron physiology and development depend on a continuous and tightly regulated trophic support from a variety of cellular sources. Trophic factors guide the generation and positioning of motor neurons during every stage of the developmental process. As well, they are involved in axon guidance and synapse formation. Even in the adult spinal cord an uninterrupted trophic input is required to maintain neuronal functioning and protection from noxious stimuli. Among the trophic factors that have been demonstrated to participate in motor neuron physiology are vascular endothelial growth factor (VEGF), glial-derived neurotrophic factor (GDNF), ciliary neurotrophic factor (CNTF) and insulin-like growth factor 1 (IGF-1). Upon binding to membrane receptors expressed in motor neurons or neighboring glia, these trophic factors activate intracellular signaling pathways that promote cell survival and have protective action on motor neurons, in both in vivo and in vitro models of neuronal degeneration. For these reasons these factors have been considered a promising therapeutic method for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases, although their efficacy in human clinical trials have not yet shown the expected protection. In this minireview we summarize experimental data on the role of these trophic factors in motor neuron function and survival, as well as their mechanisms of action. We also briefly discuss the potential therapeutic use of the trophic factors and why these therapies may have not been yet successful in the clinical use.
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spelling pubmed-39375892014-03-10 Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy Tovar-y-Romo, Luis B. Ramírez-Jarquín, Uri Nimrod Lazo-Gómez, Rafael Tapia, Ricardo Front Cell Neurosci Neuroscience Motor neuron physiology and development depend on a continuous and tightly regulated trophic support from a variety of cellular sources. Trophic factors guide the generation and positioning of motor neurons during every stage of the developmental process. As well, they are involved in axon guidance and synapse formation. Even in the adult spinal cord an uninterrupted trophic input is required to maintain neuronal functioning and protection from noxious stimuli. Among the trophic factors that have been demonstrated to participate in motor neuron physiology are vascular endothelial growth factor (VEGF), glial-derived neurotrophic factor (GDNF), ciliary neurotrophic factor (CNTF) and insulin-like growth factor 1 (IGF-1). Upon binding to membrane receptors expressed in motor neurons or neighboring glia, these trophic factors activate intracellular signaling pathways that promote cell survival and have protective action on motor neurons, in both in vivo and in vitro models of neuronal degeneration. For these reasons these factors have been considered a promising therapeutic method for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases, although their efficacy in human clinical trials have not yet shown the expected protection. In this minireview we summarize experimental data on the role of these trophic factors in motor neuron function and survival, as well as their mechanisms of action. We also briefly discuss the potential therapeutic use of the trophic factors and why these therapies may have not been yet successful in the clinical use. Frontiers Media S.A. 2014-02-28 /pmc/articles/PMC3937589/ /pubmed/24616665 http://dx.doi.org/10.3389/fncel.2014.00061 Text en Copyright © 2014 Tovar-y-Romo, Ramírez-Jarquín, Lazo-Gómez and Tapia. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Tovar-y-Romo, Luis B.
Ramírez-Jarquín, Uri Nimrod
Lazo-Gómez, Rafael
Tapia, Ricardo
Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title_full Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title_fullStr Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title_full_unstemmed Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title_short Trophic factors as modulators of motor neuron physiology and survival: implications for ALS therapy
title_sort trophic factors as modulators of motor neuron physiology and survival: implications for als therapy
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937589/
https://www.ncbi.nlm.nih.gov/pubmed/24616665
http://dx.doi.org/10.3389/fncel.2014.00061
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